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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

5-bromo-2-(difluoromethyl)pyrimidine

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Chemical Name: 5-bromo-2-(difluoromethyl)pyrimidine
CAS Number: 1780834-92-5
Product Number: AG01DYWB(AG01DYWB)
Synonyms:
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Molecular Formula:
Molecular Weight:

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Chemical Structure


5-Bromo-2-(difluoromethyl)pyrimidine is a versatile building block commonly utilized in chemical synthesis due to its unique structural properties. This compound serves as a valuable intermediate in the formation of various pharmaceuticals, agrochemicals, and fine chemicals. Its ability to react with different functional groups allows for the introduction of new chemical moieties, enabling the synthesis of complex molecules with specific biological activities. In addition, 5-Bromo-2-(difluoromethyl)pyrimidine can participate in cross-coupling reactions, nucleophilic substitutions, and other key transformations, making it an essential component in the creation of diverse chemical compounds. Its reactivity, selectivity, and compatibility with a wide range of reaction conditions make it a valuable tool for synthetic chemists seeking efficient and reliable methods for constructing molecular structures with tailored properties.